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Anti-Human CD34 FITC

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  • ¥1188
  • ebioscience
  • 11-0349-41
  • 2025年07月09日
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    • 文献和实验
    • 技术资料
    • 抗体英文名

      Anti-Human CD34 FITC

    • 规格

      25tests

    The 4H11 monoclonal antibody reacts with human CD34, also known as mucosialin. CD34 belongs
    to a protein family which also includes endoglycan and podocalyxin. Members of this family
    are single pass transmembrane proteins with a heavily glycosylated extracellular and N-terminal
    mucin domain. CD34 was first identified as an antigen expressed on hematopoietic progenitors,
    and has since been extensively used as a marker to isolate cells capable of hematopoietic cell
    engraftment. In spite of this, the function of CD34 remains unresolved. In addition to expression
    on hematopoietic progenitors, CD34 is expressed on some populations of mesenchymal stem cells,
    tumor cell lines, and by vascular endothelia in the adult. Epitopes of CD34 have been assigned to
    three classes (class I, II or III) based on their differential sensitivity to enzymatic cleavage
    by neuraminidase, chymopapain, or O-glycoprotease. According to this analysis, the 4H11 antibody
    belongs to class III, indicating that it reacts with a protein epitope.
    Data for Anti-Human CD34 FITC.

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    相关实验
    • Transmigration of Human CD34+ Cells

      to understand the mechanisms responsible for their homing and/or mobilization. In this chapter, we will describe the methodology utilized in our laboratory to evaluate migration of human CD34+ cells that contain HSC.

    • Generation of TransgenicT Cells from Human CD34+Cord Blood Cells

      Hematopoietic stem cells (HSCs), progenitor cells capable of generating all peripheral blood cell lineages, are believed not to express lineage markers (Lin) found on the latter, nor CD38, but may or may not express CD34. Besides HSCs

    • Short-Term Culture of Human CD34+ Cells for Lentiviral Gene Transfer

      biological properties of HSCs. We describe here methods for short-term ex vivo culture and gene transfer into human HSCs. Cord blood-derived HSC gene transfer can be tuned to limit the average level of vector integration or instead to maximize

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